Medical device recalls Moderate risk

McKesson Technologies, Inc. recalls Paragon Laboratory Management

Recall date
June 15, 2014
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-2263-2015
FDA classification
Class II
Brand / firm
McKesson Technologies, Inc.
Sold / distributed
Nationwide Distribution including Puerto Rico and to the states of : CA, CO., CT, FL, GA, ID, IL, IN, IA, KS, KY, LA, ME, MD, MA, MI, MN, MS, MO, MT, NE, NH, NJ, NM, NY, NC, OH, OK, OA, PA, SC, SD, TN, TX, VT, VA, WV and WY.

Why it was recalled

For Paragon Laboratory Management 12.1 and 12.1.1 releases, if used with Microsoft SQL Server 2012, the Final Cumulative Report may incorrectly display the data.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Paragon Laboratory Management

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